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Trudell Medical Group

Senior Product Development Engineering Specialist - Design Support & Sustaining

London, ON, Canada

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Job details

Experience: 10-15 years of product development and design experience =
Posting language: English
Posted: Oct 30, 2026

Original job description

At Trudell Medical International (TMI), we pride ourselves on our passion for finding innovative and creative solutions which has enabled us to develop medical devices that continue to make a difference in the lives of people around the world. Situated within a modern facility located in beautiful London, Ontario, TMI offers a comfortable work environment with a respectful and family-oriented culture.

As an employee of Trudell Medical International, not only will you contribute to the development of products at the cutting edge of medical device technology, but you will also have the opportunity to perform challenging work alongside a first-rate group of dedicated professionals.

We’re actively searching for our next team member for the position of:

SENIOR PRODUCT DEVELOPMENT ENGINEERING SPECIALIST – DESIGN SUPPORT & SUSTAINING

Job Purpose

Deliver on complex and/or multiple innovative medical device designs that provide exceptional value to our patients. Demonstrate expert proficiency with the tools and techniques of medical device design while mentoring less experienced engineers. Influence cross functional teams to deliver new product development projects on plan, within target costs, and that meet or exceed our expectations for quality and innovation.

Responsibilities Include:

DESIGN DEVELOPMENT & TESTING

Design efficient and effective mechanical and electromechanical systems and sub-systems to support product design. Acting as design responsible engineer (DRE) or as an advisor to more junior Engineers
Actively mentor less experienced engineers to improve their capability and optimize the delivery of medical device designs
Develop and maintain internal and external networks that can be leveraged to advance product development capabilities

DEVELOPMENT PROCESS

Lead and/or advise on multiple different invention disclosures including for new technologies or systems

Lead and/or advise on development of multiple project plans and/or where planning expertise is required to address deep uncertainty or new areas of development
Lead continuous improvement teams and deliver on continuous improvement initiatives that improve aspects of the new product development process
Initiate lessons learned processes at points during the product development process in order to capture opportunities for improvement

COLLABORATION

Collaboration with the SEED team to transfer product ideas into Phase 1 of product development
Collaborate with the Marketing and Sales department to investigate incremental business ideas to capture the voice of the customer and develop a business case for strategic review

REGULATORY & POLICY

Deliver development of complicated products and/or systems to achieve regulatory clearance and policy compliance
Identify opportunities for improvement to regulatory related activities to optimize product development and improve effectiveness

health & Safety

Comply with relevant health and safety legislation, including the Workplace Safety and Insurance Act, the Occupational Health and Safety Act, etc.
Identify areas for improvement with regards to Health and Safety within product development

QUALIFICATIONS

Degree in Engineering (Mechanical, Mechatronic, Biomedical) or a related field of study
10-15 years of product development and design experience =
Experience working in a regulated industry an asset, e.g. medical device, pharmaceutical or aerospace

CAD (Parts, Assemblies, Drawings, PDM, etc.)
Analysis skills (Risk, Tolerances, Statistical, Root Cause, etc.)
Modelling and Simulation (FEA, CFD, Mathematical, etc.)
Design Verification and Validation (Test Design, Functional, Usability, Compliance, etc.)
Design for Manufacture (molding, automated assembly, packaging, etc.)
Prototyping (3D Printing, Electronics, Traditional, etc.)
Programming (Python, Matlab, Arduino, etc.)
Knowledge with electronics (prototype PCB or breadboard, component selection, test, etc.)
Leadership and Mentoring skills

Project management experience

At an applicant’s request, TMI will make accommodation to its recruitment process to meet the needs of applicants with disabilities.

Trudell Medical International is committed to providing fair and equitable compensation opportunities to all teammates. The range displayed on each job posting reflects the target for new hire salaries for the advertised position. Within the range, individual compensation is determined by job-related skills and knowledge, relevant professional, lived experience, and/or work location. Our compensation policies and practices are designed to allow our colleagues’ growth and salary progression as they develop in their role. As a candidate, you are encouraged to ask compensation-related questions and have an open dialogue with your recruiter, who can provide specific details for this role and share more information about our total rewards package.

As part of our recruitment process, we may use AI tools to screen applicants and assist in evaluating candidate qualifications. All final hiring decisions are made by our recruitment team.

We are an equal opportunity employer and it is important to our Company that all its employees, including those with disabilities, find our workplace to be welcoming and supportive. If you are a candidate with a disability who requires accommodations during the recruitment process, please let us know.

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More about this job

Responsibilities

The specialist will lead complex medical device design projects while mentoring junior engineers to ensure high-quality, innovative product development. They are responsible for collaborating with cross-functional teams to meet regulatory requirements and drive continuous improvement initiatives throughout the development process.

Requirements

Candidates must possess a degree in Engineering and 10-15 years of experience in product development and design, preferably within a regulated industry. Proficiency in CAD, simulation tools, and design verification processes is essential for this senior-level role.

Skills

Mechanical engineering
Mechatronics
Biomedical engineering
Medical device design
CAD
Risk analysis
Statistical analysis
Root cause analysis
FEA
CFD
Design verification
Design validation
Design for manufacture
Prototyping
Python
Matlab

Visa sponsorship

Not detected in the job text

Keywords

Medical devices
Product development
Mechanical systems
Electromechanical systems
Design responsible engineer
Regulatory clearance
Compliance
FEA
CFD
3D printing
Arduino
PCB
Project management
Root cause analysis
Tolerance analysis
Risk management
Continuous improvement
Voice of the customer
Phase 1 development
Engineering
Mechatronics
Biomedical
CAD
PDM
Python
Matlab
Manufacturing
Packaging
Design verification
Design validation

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